Acetic Acid → 3-(2-(4-(1-Methylethyl)-2-thiazolyl)ethenyl)benzaldehyde
反応式
[CH3:1][CH:2]([C:4]1[N:5]=[C:6]([CH3:9])[S:7][CH:8]=1)[CH3:3].C(O[C:14](=[O:16])[CH3:15])(=O)C.C(O)(=O)C.[C:21]1([CH3:27])[CH:26]=C[CH:24]=[CH:23][CH:22]=1>>[CH3:1][CH:2]([C:4]1[N:5]=[C:6]([CH:9]=[CH:27][C:21]2[CH:26]=[C:15]([CH:24]=[CH:23][CH:22]=2)[CH:14]=[O:16])[S:7][CH:8]=1)[CH3:3]参加物
5
実験手順
4-(1-Methylethyl)-2-methylthiazole (546 mg, EP 0219436 p. 19) and isophthaladehyde (570 mg, 1.1 equiv.) are heated at reflux in acetic anhydride (1.1 mL, 3 equiv.) 16 hours. The reaction mixture is cooled and the acetic acid and anhydride are co-evaporated with toluene. The title compound is purified by flash chromatography on silica using EtOAc:hexane 10:90.
後処理
- temperatureThe reaction mixture is cooled
- customThe title compound is purified by flash chromatography on silica
出典と根拠
- ORDレコード
- ord-c88d99a0ca7245358ebb6512e838011e
- 出典データセット
- uspto-grants-1990_10
- 特許番号
- US04962117
反応ノート
読み込み中…